{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Broomfield",
      "address_1": "310 Interlocken Pkwy",
      "reason_for_recall": "Zimmer Biomet is recalling the Altius M-INI OCT Posterior Spinal Fixation System because the driver is unable to mate with the screw head tulip.",
      "address_2": "Suite 120",
      "product_quantity": "141",
      "code_info": "505951,M16562R01,505951,510710,510981,514814,533566,536398,543663,546565,546566,549528,565465,565464,567525,",
      "center_classification_date": "20170328",
      "distribution_pattern": "Worldwide Distribution - US (nationwide) and Internationally to the Netherlands",
      "state": "CO",
      "product_description": "Altius M-INI OCT Posterior Spinal Fixation System, Model Number 1200-9216  The AltiusTM OCT and AltiusTM M-INITM OCT Systems when intended to promote fusion of the cervical spine and occipitocervico-thoracic junction (Occiput-T3), these systems are indicated for: DDD (neck pain of discogenic origin with degeneration of the disc as confirmed by patient history and radiographic studies); spondylolisthesis; spinal stenosis; fracture/dislocation; atlantoaxial fracture with instability; occipitocervical dislocation; revision of previous cervical spine surgery; and tumors. The occipital bone screws are limited to occipital fixation only",
      "report_date": "20170405",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Zimmer Biomet Spine, Inc",
      "recall_number": "Z-1691-2017",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "76610",
      "termination_date": "20180730",
      "more_code_info": "",
      "recall_initiation_date": "20170316",
      "postal_code": "80021-3479",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}